Posttraumatic Stress Disorder Clinical Trial
Official title:
Evaluation of ProVetus/Sponsorship Initiative
Verified date | April 2018 |
Source | Teachers College, Columbia University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Some Veterans who recently served in the military report significant psychological problems based on their experiences in the military. Stressors that these Veterans face when they transition out of the military can acerbate these problems and negatively impact their long-term physical and psychological well-being. The investigators are conducting a randomized controlled trial to evaluate the efficacy of providing Veterans who are transitioning back into their civilian communities trained, peer mentorship (Pro Vetus) and membership in a Veteran Support Organization (VSO) Team Red, White, and Blue (TM RWB) to reduce transition stressors, maintain psychological and physical health, reduce suicides and reduce criminal incidents.
Status | Completed |
Enrollment | 203 |
Est. completion date | July 2017 |
Est. primary completion date | July 2017 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Aged 18 and over, prior military service within the last twelve years, and currently reside within the NYC area (and anticipate staying within the area for at least one year) or will move to NYC area prior to December 2016 (and anticipate staying for at least one year). Exclusion Criteria: - Previous membership within Team Red, White, and Blue. |
Country | Name | City | State |
---|---|---|---|
United States | Teachers College, Columbia University | New York | New York |
Lead Sponsor | Collaborator |
---|---|
Teachers College, Columbia University |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in baseline PCL (PTSD) scores across 3 timepoints | Baseline, 3 months after, 10 months after, 16 months after | ||
Primary | Change in baseline Military to Civilian Questionnaire scores across 3 timepoints | Baseline, 3 months after, 10 months after, 16 months after | ||
Primary | Change in baseline Social Support Scale scores across 3 timepoints | Baseline, 3 months after, 10 months after, 16 months after | ||
Primary | Change in baseline suicidality across 2 timepoints | Outcome measured through Mortality (Suicide) Data Center for Disease Control | 16 months after baseline and 5 years after baseline | |
Secondary | Change in baseline Veteran Rand 36 scores across 3 timepoints | Baseline, 3 months after, 10 months after, 16 months after | ||
Secondary | Change in baseline PHQ-15 scores across 3 time points | Baseline, 3 months after, 10 months after, 16 months after | ||
Secondary | Change in baseline Criminal Background Record across 3 timepoints | Baseline, 3 months after, 10 months after, 16 months after | ||
Secondary | Change in baseline Criminal Background Self-Report across 3 timepoints | Baseline, 3 months after, 10 months after, 16 months after | ||
Secondary | Change in baseline AUDIT-C (Alcohol Use) scores across 3 time points | Baseline, 3 months after, 10 months after, 16 months after | ||
Secondary | Change in baseline Quality of Life, Enjoyment and Satisfaction scores across 3 time points | Baseline, 3 months after, 10 months after, 16 months after | ||
Secondary | Change in baseline Social Adjustment Scale scores across 3 time points | Baseline, 3 months after, 10 months after, 16 months after |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT03384706 -
A Comparison of CPT Versus ART Versus WL
|
N/A | |
Completed |
NCT03418129 -
Neuromodulatory Treatments for Pain Management in TBI
|
N/A | |
Completed |
NCT03129204 -
Sensation Awareness Focused Training for Spouses
|
N/A | |
Recruiting |
NCT05651295 -
A Precision Medicine Approach to Target Engagement for Emotion Regulation
|
N/A | |
Completed |
NCT05113277 -
Development and Evaluation of a Tonic Immobility Focused Psychoeducational Intervention
|
N/A | |
Recruiting |
NCT05327504 -
Written Exposure Therapy for Veterans With SUD and PTSD
|
N/A | |
Recruiting |
NCT05843695 -
Enhancing Psychotherapy for Veterans and Service Members With PTSD and Anxiety
|
N/A | |
Active, not recruiting |
NCT05530642 -
An Augmented Training Program for Preventing Post-Traumatic Stress Injuries Among Diverse Public Safety Personnel
|
N/A | |
Completed |
NCT00644423 -
Omega-3 Fatty Acids and Post Traumatic Stress Disorder (PTSD)
|
N/A | |
Completed |
NCT02989987 -
NET for SGBV Survivors in Eastern DR Congo
|
N/A | |
Completed |
NCT02320799 -
Randomized Controlled Trial of Interpersonal Psychotherapy for Depression and PTSD Among HIV+ Women in Kenya
|
N/A | |
Recruiting |
NCT02293291 -
Thermal Clinic Treatment in Gulf War Illness
|
Phase 1/Phase 2 | |
Completed |
NCT02242136 -
Treatment of Posttraumatic Stress Disorder and Aggressive Behavior in Soldiers and Ex-combatants
|
N/A | |
Completed |
NCT02720497 -
The Efficacy of 90-Minute Versus 60-Minute Sessions of Prolonged Exposure for PTSD
|
N/A | |
Completed |
NCT01911585 -
Efficacy of 60-minute Versus 90-minute Sessions in Treating PTSD Using Prolonged Exposure
|
N/A | |
Terminated |
NCT01408641 -
Topiramate for Alcohol Use in Posttraumatic Stress Disorder
|
N/A | |
Completed |
NCT01693978 -
Contingency Outcomes in Prolonged Exposure
|
N/A | |
Completed |
NCT01469754 -
Longitudinal Survey Analysis in Lymphoma Survivors
|
N/A | |
Completed |
NCT02362477 -
Telemental Health and Cognitive Processing Therapy for Female Veterans With Military-related PTSD
|
Phase 3 | |
Terminated |
NCT01239173 -
Emotional Memory Reactivation in Posttraumatic Stress Disorder
|
Phase 3 |